The degradation behavior of ethyl xanthate(EX) salt was the most widely used collector in sulfide mineral flotation and emission of flotation tailings with residual EX was harmful to environment. In this work, hydroge...The degradation behavior of ethyl xanthate(EX) salt was the most widely used collector in sulfide mineral flotation and emission of flotation tailings with residual EX was harmful to environment. In this work, hydrogen peroxide(H2O2) was investigated by UV-visible spectroscopy(UV/Vis) at different p H values from 3 to 12. For p H value from 5 to 12, EX was oxidized into ethyl per xanthate(EPX) by H2O2. Then EPX was further oxidized into thiosulfate(TS) salt rather than ethyl thiocarbonate(ETC) and this step was the reaction-limited step. Then depending on p H values, TS was degraded into sulphate and carbonate salts(p H>7) or elemental sulfur(p H<7). The kinetics data show that the degradation rate of EX increases with increasing the H2O2 concentration and is independent on the p H values. Without H2O2, EX is hydrolyzed to carbon disulfide fast at p H value <3.0, but the reaction of hydrolysis is undetectable at p H value >3.0 during test time.展开更多
In this paper, environmental scanning electron microscopy （ESEM） is applied to characterizing the mineral and element distribution of chromite ore processing residue （COPR）. The test results show that Cr-bearing b...In this paper, environmental scanning electron microscopy （ESEM） is applied to characterizing the mineral and element distribution of chromite ore processing residue （COPR）. The test results show that Cr-bearing brownmillerite occurs in the rim of COPR particle, while hydroandradite with Cr （Ⅵ） in its structure presents inside the COPR particle. Periclase and calcite occur in the interstitial area. Element analyses show that Ca, Fe and Al are distributed throughout the COPR particle, and Mg exists mostly in the interstitial area or on the particle surface. A lower content of Cr is evenly distributed in the COPR particle, while slightly higher concentration of Cr occurs inside the particle. It is suggested that it will take a relatively longer time for Cr to migrate out of COPR, especially fbr hexavalent chromium, so the leaching time and the particle size may be two important factors to affect the release of Cr （Ⅵ）.展开更多
基金Project(2013AA064102)supported by the National High Technology Research and Development Program of ChinaProject(B14034)supported by the Program of Introducing Talents of Discipline to Universities,ChinaProject supported by the 2011 Collaborative Innovation Center for Clean and Efficient utilization of Strategic Metal Mineral Resources,China
文摘The degradation behavior of ethyl xanthate(EX) salt was the most widely used collector in sulfide mineral flotation and emission of flotation tailings with residual EX was harmful to environment. In this work, hydrogen peroxide(H2O2) was investigated by UV-visible spectroscopy(UV/Vis) at different p H values from 3 to 12. For p H value from 5 to 12, EX was oxidized into ethyl per xanthate(EPX) by H2O2. Then EPX was further oxidized into thiosulfate(TS) salt rather than ethyl thiocarbonate(ETC) and this step was the reaction-limited step. Then depending on p H values, TS was degraded into sulphate and carbonate salts(p H>7) or elemental sulfur(p H<7). The kinetics data show that the degradation rate of EX increases with increasing the H2O2 concentration and is independent on the p H values. Without H2O2, EX is hydrolyzed to carbon disulfide fast at p H value <3.0, but the reaction of hydrolysis is undetectable at p H value >3.0 during test time.
基金Supported by National Natural Science Foundation of China (No. 50808091)
文摘In this paper, environmental scanning electron microscopy （ESEM） is applied to characterizing the mineral and element distribution of chromite ore processing residue （COPR）. The test results show that Cr-bearing brownmillerite occurs in the rim of COPR particle, while hydroandradite with Cr （Ⅵ） in its structure presents inside the COPR particle. Periclase and calcite occur in the interstitial area. Element analyses show that Ca, Fe and Al are distributed throughout the COPR particle, and Mg exists mostly in the interstitial area or on the particle surface. A lower content of Cr is evenly distributed in the COPR particle, while slightly higher concentration of Cr occurs inside the particle. It is suggested that it will take a relatively longer time for Cr to migrate out of COPR, especially fbr hexavalent chromium, so the leaching time and the particle size may be two important factors to affect the release of Cr （Ⅵ）.
